Guidelines for the diagnosis and management of hereditary spherocytosis–2011 update

PHB Bolton‐Maggs, JC Langer… - British journal of …, 2012 - Wiley Online Library
Guidelines on hereditary spherocytosis (HS) published in 2004 (Bolton‐Maggs et al, 2004)
are here replaced to reflect changes in current opinion on the surgical management …

Rapid flow cytometric test for the diagnosis of membrane cytoskeleton‐associated haemolytic anaemia

MJ King, J Behrens, C Rogers, C Flynn… - British journal of …, 2000 - Wiley Online Library
The flow cytometric test measures the fluorescence intensity of intact red cells labelled with
the dye eosin‐5‐maleimide, which reacts covalently with Lys‐430 on the first extracellular …

Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1

LJ Bruce, HC Robinson, H Guizouarn, F Borgese… - Nature …, 2005 - nature.com
We identified 11 human pedigrees with dominantly inherited hemolytic anemias in both the
hereditary stomatocytosis and spherocytosis classes. Affected individuals in these families …

Absence of CD47 in protein 4.2–deficient hereditary spherocytosis in man: an interaction between the Rh complex and the band 3 complex: Presented at the 43rd …

LJ Bruce, S Ghosh, MJ King, DM Layton… - Blood, The Journal …, 2002 - ashpublications.org
We present data on a patient of South Asian origin with recessive hereditary spherocytosis
(HS) due to absence of protein 4.2 [4.2 (−) HS]. Protein 4.2 cDNA sequence analysis …

Eosin‐5‐maleimide binding to band 3 and Rh‐related proteins forms the basis of a screening test for hereditary spherocytosis

MJ King, JS Smythe, R Mushens - British journal of …, 2004 - Wiley Online Library
Flow cytometric analysis of eosin‐5‐maleimide (EMA) binding to red cells is a screening test
for the diagnosis of hereditary spherocytosis (HS). The present study used chemical …

Blood group antigens on human erythrocytes-distribution, structure and possible functions

MJ King - Biochimica et Biophysica Acta (BBA)-Reviews on …, 1994 - Elsevier
Human erythrocyte blood group antigens can be broadly divided into carbohydrates and
proteins. The carbohydrate-dependent antigens (eg, ABH, Lewies, Ii, P1, P-related, T and …

Using the eosin‐5‐maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis

MJ King, P Telfer, H MacKinnon… - Cytometry Part B …, 2008 - Wiley Online Library
Background: Flow cytometric analysis of eosin‐5‐maleimide (EMA)‐labeled red blood cells
(RBCs) has been used as a screening test for the diagnosis of patients with hereditary …

Toward the harmonization of result presentation for the eosin‐5′‐maleimide binding test in the diagnosis of hereditary spherocytosis

L Hunt, D Greenwood, H Heimpel… - Cytometry Part B …, 2015 - Wiley Online Library
Background The eosin‐5′‐maleimide (EMA) Binding test measures reduced mean
channel fluorescence (MCF) reading of EMA‐labeled red cells (EMA‐RBCs) from patients …

Phenotype and mRNA expression of syncytiotrophoblast microparticles isolated from human placenta

B Kumpel, MJ King, S Sooranna… - Annals of the New …, 2008 - Wiley Online Library
Fetal and neonatal alloimmune thromboctyopenia due to maternal human platelet antigen
(HPA)‐1a antibodies affects primigravidas. Immunization must occur early in pregnancy …

Two different glycosyltransferase defects that result in GalNAcα-O-peptide (Tn) expression

MJ King, A Chan, R Roe, BF Warren, A Dell, HR Morris… - 1994 - academic.oup.com
This study shows for the first time that different glycosyltransferase defects in the
biosynthesis of O-linked oligosaccharides give rise to the same GalNAcα-O-Ser/Thr …